Furosemide
- Product NDC
- 63629-1214
- 11-digit product format
- 636291214
- Labeler code
- 63629
- Product ID
- 63629-1214_ddf690b2-6661-4f06-af84-322d335fa74b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 63629-1214_ddf690b2-6661-4f06-af84-322d335fa74b
- SPL ID
- ddf690b2-6661-4f06-af84-322d335fa74b
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Furosemide
- Generic name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Marketing start
- 2004-03-26
- Marketing category
- ANDA
- Application number
- ANDA076796
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| FUROSEMIDE | 20 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 310429 |
| Spl Set Id | 3ad12e70-3c2e-44af-bb6b-5762d181c76b |
| Manufacturer Name | Bryant Ranch Prepack |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 63629-1214-1 | 1000 TABLET in 1 BOTTLE (63629-1214-1) | 2021-01-14 | No |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7LXU5N7ZO5 | FUROSEMIDE | 54-31-9 | FUROSEMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-1214-1 | 63629121401 | 1000 TABLET in 1 BOTTLE (63629-1214-1) | 1000 tablet | 2021-01-14 | No | No | Historical |